反应 #1543043

ord-0f60be9708fd4d5da0b2bd4e47181571

反应方程式

CS(=O)(=O)c1ccc(C(=O)Cl)c(Cl)c1
2-chloro-4-methylsulfonylbenzoyl chloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
ClC(Cl)C(Cl)Cl
1,1,2,2-tetrachloroethane
Cl
hydrochloric acid
CS(=O)(=O)c1ccc(C(=O)c2c(O)cc(Cl)cc2Cl)c(Cl)c1
2,2', 4'-Trichloro-6'-hydroxy-4-methylsulfonylbenzophenone

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the mixture is subsequently refluxed for 7 hours
  2. 2
    其他The organic phase is removed
  3. 3
    萃取the aqueous phase is extracted twice
  4. 4
    洗涤The combined organic phases are washed until neutral and
  5. 5
    萃取subsequently extracted three times
  6. 6
    过滤The precipitate is filtered off
  7. 7
    洗涤washed with water until neutral and
  8. 8
    其他dried

实验过程

3.00 g of 2-chloro-4-methylsulfonylbenzoyl chloride are added in portions at room temperature to a mixture of 1.97 g of 3,5-dichlorophenone and 3.23 g of aluminum chloride in 50 ml of 1,1,2,2-tetrachloroethane, and the mixture is subsequently refluxed for 7 hours. When cold, the reaction mixture is poured onto 100 g of ice and 20 ml of concentrated hydrochloric acid. The organic phase is removed, and the aqueous phase is extracted twice using 50 ml of dichloromethane. The combined organic phases are washed until neutral and subsequently extracted three times using in each case 25 ml of 2N sodium hydroxide solution. The combined alkaline extracts are brought to a pH of 2 using concentrated hydrochloric acid. The precipitate is filtered off, washed with water until neutral and dried. This gives 3.194 g (70% of theory) of 2,2', 4'-trichloro-6'-hydroxy-4-methylsulfonylbenzophenone in the form of colorless crystals with a melting point of 123°-126° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05843869uspto-grants-1998_12